Department of Gastroenterology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Department of Pharmacology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
United European Gastroenterol J. 2021 Mar;9(2):159-176. doi: 10.1177/2050640620972602. Epub 2021 Mar 23.
The risk of severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) infection and clinical outcomes of coronavirus disease (COVID-19) in inflammatory bowel disease are unclear.
We searched PubMed and Embase with the keywords: inflammatory bowel disease, Crohn's disease, ulcerative colitis and COVID-19, novel coronavirus and SARS-CoV-2. We included studies reporting the frequency of COVID-19 infection and outcomes (hospitalisation, need for intensive care unit care and mortality) in patients with inflammatory bowel disease. We estimated the pooled incidence of COVID-19 in inflammatory bowel disease and comparative risk vis-a-vis the general population. We also estimated the pooled frequency of outcomes and compared them in patients who received and did not receive drugs for inflammatory bowel disease.
Twenty-four studies were included. The pooled incidence rate of COVID-19 per 1000 patients of inflammatory bowel disease and the general population were 4.02 (95% confidence interval [CI, 1.44-11.17]) and 6.59 [3.25-13.35], respectively, with no increase in relative risk (0.47, 0.18-1.26) in inflammatory bowel disease. The relative risk of the acquisition of COVID-19 was not different between ulcerative colitis and Crohn's disease (1.03, 0.62-1.71). The pooled proportion of COVID-19-positive inflammatory bowel disease patients requiring hospitalisation and intensive care unit care was 27.29% and 5.33% while pooled mortality was 4.27%. The risk of adverse outcomes was higher in ulcerative colitis compared to Crohn's disease. The relative risks of hospitalisation, intensive care unit admission and mortality were lower for patients on biological agents (0.34, 0.19-0.61; 0.49, 0.33-0.72 and 0.22, 0.13-0.38, respectively) but higher with steroids (1.99, 1.64-2.40; 3.41, 2.28-5.11 and 2.70, 1.61-4.55) or 5-aminosalicylate (1.59, 1.39-1.82; 2.38, 1.26-4.48 and 2.62, 1.67-4.11) use.
SARS-CoV-2 infection risk in patients with inflammatory bowel disease is comparable to the general population. Outcomes of COVID-19-positive inflammatory bowel disease patients are worse in ulcerative colitis, those on steroids or 5-aminosalicylates but outcomes are better with biological agents.
严重急性呼吸综合征相关冠状病毒 2(SARS-CoV-2)感染的风险和冠状病毒病(COVID-19)的临床结果在炎症性肠病中尚不清楚。
我们使用关键词在 PubMed 和 Embase 上进行了搜索:炎症性肠病、克罗恩病、溃疡性结肠炎和 COVID-19、新型冠状病毒和 SARS-CoV-2。我们纳入了报告炎症性肠病患者 COVID-19 感染频率和结局(住院、需要重症监护病房护理和死亡率)的研究。我们估计了炎症性肠病患者 COVID-19 的总发病率,并与普通人群进行了比较风险。我们还估计了接受和未接受炎症性肠病药物治疗的患者的结局频率,并对其进行了比较。
纳入了 24 项研究。炎症性肠病患者每 1000 例 COVID-19 的发病率和普通人群分别为 4.02(95%置信区间[CI],1.44-11.17)和 6.59[3.25-13.35],相对风险无增加(0.47,0.18-1.26)。溃疡性结肠炎和克罗恩病患者 COVID-19 的发病风险无差异(1.03,0.62-1.71)。COVID-19 阳性炎症性肠病患者需要住院和入住重症监护病房的比例分别为 27.29%和 5.33%,而死亡率为 4.27%。与克罗恩病相比,溃疡性结肠炎患者发生不良结局的风险更高。住院、重症监护病房入院和死亡的相对风险分别在接受生物制剂治疗的患者中较低(0.34,0.19-0.61;0.49,0.33-0.72 和 0.22,0.13-0.38),而在接受皮质类固醇或 5-氨基水杨酸治疗的患者中较高(1.99,1.64-2.40;3.41,2.28-5.11 和 2.70,1.61-4.55)。
炎症性肠病患者 SARS-CoV-2 感染风险与普通人群相当。COVID-19 阳性炎症性肠病患者的结局在溃疡性结肠炎患者中更差,在接受皮质类固醇或 5-氨基水杨酸治疗的患者中更差,但在接受生物制剂治疗的患者中更好。